hereditary
268 results
1 - 100- hereditary
- hereditary thrombophilia
- hereditary ferritinopathy
- hereditary aceruloplasminemia
- stomatocytosis, hereditary
- hereditary xerocytosis
- coproporphyria, hereditary coproporphyria
- hereditary arthro-ophthalmopathy, hereditary progressive arthro-ophthalmopathy
- disease
- chorea
- nephritis
- deafness
- angioedema
- elliptocytosis
- paraplegia
- cancer
- telangiectasia, telangiectasis
- impairment
- dystrophy
- dysplasia
- spherocytosis
- icatibant
- genodermatosis
- xerocyte
- Aldolase
- lanadelumab
- heritable
- ecallantide
- inotersen
- patisiran
- neuropathy
- plasmagene
- acquired
- Leber, Theodor
- index case
- myopathy
- Marie, Pierre
- multiallelic
- Troyer syndrome
- Upshaw-Schulman Syndrome
- C1-esterase inhibitor, recombinant
- dentinogenesis
- C1-esterase inhibitor
- danazol
- arthrodysplasia
- dessicocytosis
- Milroy disease
- Pyruvate Kinase
- Gastric Cancer
- C1 inhibitor (human)
- antithrombin (human)
- Rendu-Osler-Weber syndrome
- oligodontia
- transgenic
- dysostosis
- pharmacogenetics
- stomatocyte
- histidinemia
- Biopsy, Bone Marrow
- uridine triacetate
- poliosis
- cystathioninuria
- Ham Test for Paroxysmal Nocturnal Hemoglobinuria
- anemia
- osteopoikilosis
- methemoglobinemia
- Glucose-6-Phosphate Dehydrogenase
- deficiency
- exostosis
- Alpha₁-Antitrypsin and Alpha₁-Antitrypsin Phenotyping
- strain (1)
- Leri pleonosteosis
- genotype
- Subdural Hematoma
- Kartagener syndrome
- Thyroxine-Binding Globulin
- oculocerebrorenal syndrome
- Complement, Total, C3, and C4
- chondrodysplasia
- cystinuria
- acrokeratosis verruciformis
- Hydronephrosis
- oxalosis
- autohemolysis test
- penetrance
- Brugada syndrome
- abaloparatide
- pseudohypoparathyroidism
- handedness